The yellow-faced honeyeater (Caligavis chrysops) is a medium-small bird in the honeyeater family Meliphagidae. It takes both its common name and scientific name from the distinctive yellow stripes on the sides of its head. It has a loud clear call, and is one of the first birds heard in the morning. It is widespread across eastern and south eastern Australia, in open sclerophyll forests from coastal dunes to high-altitude subalpine areas, and woodlands along creeks and rivers. Comparatively short-billed for a honeyeater, it is thought to have adapted for a diet of flies, spiders and beetles, as well as nectar and pollen from the flowers of plants such as Banksia and Grevillea, and soft fruits. It catches insects in flight as well as gleaning them from the foliage of trees and shrubs.
While some yellow-faced honeyeaters are sedentary, hundreds of thousands of them migrate northwards between March and May to spend the winter in southern Queensland and return in July and August to breed in southern New South Wales and Victoria. They form socially monogamous pairs and lay two or three eggs in a delicate cup-shaped nest. While the success rate can be low, the pairs nest several times during the breeding season.
Honeyeaters’ preferred woodland habitat is vulnerable to the effects of land clearing, grazing and weeds. However, as it is common and widespread, the yellow-faced honeyeater is considered by the IUCN to be of least concern for conservation. It is considered a pest in orchards in some areas.
The yellow-faced honeyeater was first described, and placed in the genus Sylvia, by ornithologist John Latham in his 1801 work Supplementum Indicis Ornithologici, sive Systematis Ornithologiae. The specific name chrysops is from the Greek words meaning "gold" and "face" in reference to the stripe of yellow feathers. French ornithologist Louis Jean Pierre Vieillot described it as Melithreptus gilvicapillus in 1817, and English zoologist George Robert Gray as Ptilotis trivirgata in 1869. It was classified in the genus Lichenostomus for many years until 2011.
Delineating Lichenostomus had been systematically contentious, and evaluations of relationships among honeyeaters in the genus using dense taxon and nucleotide sampling confirmed previous findings that Lichenostomus is not monophyletic. While five species have previously been described as comprising the Caligavis subgroup, studies using the mitochondrial ND2 and nuclear β-fibrinogen-7 genes identified the yellow-faced honeyeater as closely related to the black-throated honeyeater (C. subfrenatus), and the obscure honeyeater (C. obscurus) of New Guinea, and they were therefore able to be grouped in the genus Caligavis. The bridled honeyeater (B. frenatus) and the Eungella honeyeater (B. hindwoodi) were sufficiently different to be a separate genus as Bolemoreus.
Three subspecies have been described (Matthews, 1912) but are not universally recognised. There are only very slight differences between the nominate race and L.c. samueli found in the Mount Lofty Ranges in South Australia and L. c. barroni from Clarke Range and the Atherton Tableland in Queensland. The latter race is described as "poorly differentiated" and "possibly not worthy of recognition" by the Handbook of the Birds of the World.
Surgeon-General to the First Fleet John White caught one in May 1788, calling it a yellow-faced flycatcher in his Journal of a Voyage to New South Wales, which was published in 1790. Latham called it the black-cheeked honeyeater. John Gould called it the yellow-faced honeyeater in 1848, which has become its official name. It is also known as the yellow-gaped honeyeater, or the quitchup in reference to its call.
The yellow-faced honeyeater is a medium-small, greyish-brown bird that takes its common name from distinctive yellow stripes on the sides of the head. Yellow feathers form a narrow stripe above the gape, then broaden and curve below the eye to end in a small white patch of feathers on the ear-coverts. Above the yellow stripe is a black eye stripe which is broken by a small yellow to off-white patch behind the eye, and below is another distinct black stripe running the length of the yellow line. The chin and throat are a pale greyish brown, streaked with slightly darker grey, and the upper body is a dark greyish brown to olive-brown. Olive green outer edges on the remiges combine to form an olive panel on the folded wing. The bill is black and slightly down-curved, and the gape is cream. The iris is a dusky blue in adult birds, and brown in juveniles. Juveniles are very similar to the adult, with slightly less streaking on the breast, an orange-brown tip on the bill and a yellower gape; male and female birds are also similar, with the male being slightly larger; and in the field there are no visible differences between the subspecies. The yellow-faced honeyeater averages 15–17.5 centimetres (5.9–6.9 in) in length, with a wingspan of 21.5–26 centimetres (8.5–10.2 in) and a weight of between 12.5–20.5 grams (0.44–0.72 oz) (average 17 grams (0.60 oz)).
One of the first birds heard in the morning, the yellow-faced honeyeater utters calls that are full and loud, and extremely varied. The male sings from a roost for up to an hour, beginning twenty or thirty minutes before dawn. The song is a running series of cheerful notes sounding like chick-up, chick-up, from which its common name of quitchup is derived. Counter-singing by neighbouring birds is common. The territorial call, also given by opponents during fights, is a long preet with an upward inflection. The alarm call is a loud trilling whistle. Common calls, thought to be contact calls, are animated two-note calls variously described as terric, terric, cr-rook, cr-rook or put-put, put-put.
Distribution and habitat
The yellow-faced honeyeater is widespread across eastern and south eastern Australia, in open sclerophyll forests from coastal dunes to high-altitude subalpine areas, and often in riparian woodlands. It is usually found in open forests dominated by spotted gum with ironbarks and stringybarks such as Eucalyptus crebra and E. melanophloia, with a light shrubby understorey, and less often in dry open forests and woodlands dominated by Angophora, Acacia, Banksia, Casuarina or Callitris. It occurs in high-altitude, tall, open forests of alpine ash and woodlands dominated by snow gum or white box. It has been recorded in coastal heath when banksias are flowering, and amongst flowering mangroves. It occupies areas infested with weeds such as Scotch broom and blackberries, and developed areas including orchards and parks and gardens, where it feeds on cultivated fruit and flowers. It can be found in forests regenerating after fire or logging, though it is more common in mature forests. It usually avoids woodland, unless it is near forest or has an understory of scleophyll plants.
The yellow-faced honeyeater ranges across a broad arc from near Cooktown in Far North Queensland, south west between a line from Charters Towers to Albury and the coast, and then west to the Fleurieu Peninsula and Mount Lofty Ranges in South Australia. Population densities have been recorded from 0.01 birds per hectare (2.5 acres) near Armidale in New South Wales to 7.8 birds per hectare at Tarnagulla, Victoria. During the winter months of June and July, numbers are generally decreased in Victoria and increased in Queensland, following northward migration.
While there are resident populations of the yellow-faced honeyeater throughout its range, it is for the most part a seasonal, latitudinal, daytime migrant. During the autumn (March to May) it migrates north along the highlands and coastal fringe of eastern Australia to southern Queensland, to return in the spring (August to October) of the same year. The birds commonly move in flocks of 10 to 100 birds, but occasionally in larger groups of up to 1,000 or more birds. The groups can include other species such as the white-naped honeyeater, fuscous honeyeater, noisy friarbird and silvereye. They move in successive flocks at a rate of up to several thousand birds an hour. Near Hastings Point in New South Wales over 100,000 passed through in a single day. The species is able to detect geomagnetic fields and uses them to navigate while migrating. Experiments where the vertical component of the magnetic field was reversed indicate that the magnetic compass of the yellow-faced honeyeater is based on the inclination of the field lines and not on polarity, distinguishing between the direction of the equator and the poles, rather than north and south. While their flight is in one general direction, it is not in a straight line as the flocks stay in vegetated areas, negotiate gaps in the mountain ranges and detour around cities.
The migration of many birds in Australia, including honeyeaters, has generally been described as occurring mainly in response to external environmental stimuli, such as food availability or an influx of water. However, the yellow-faced honeyeater has been found to have a broad range of characteristics which are consistent with the adaptations of Northern Hemisphere migrants to their mobile lifestyle: an annual cycle of migratory restlessness; seasonally appropriate orientation based on magnetic, solar and polarised light cues; and a migration program based on the magnetic inclination compass.
The yellow-faced honeyeater is usually seen singly, in pairs or in small family groups when not migrating. While it is generally active, in the early morning it will often sit still on high perches for long periods of time.
Comparatively short-billed for a honeyeater, the yellow-faced honeyeater is thought to have adapted for a mixed diet. Its diet consists of nectar, pollen, fruit, seeds, honeydew and insects. It is arboreal, foraging primarily amongst the foliage and flowers of trees, shrubs and mistletoes, less often on branches and tree trunk, and rarely on the ground. A study of the pollen on the bills and foreheads of captured birds found that 70% carried pollen from silver banksia (Banksia marginata), 61% from heath-leaved banksia (Banksia ericifolia), and 22% carried pollen from other plants in the area including fern-leaved banksia (Banksia oblongifolia), mountain devil (Lambertia formosa) and green spider flower (Grevillea mucronulata). Of 545 observations of yellow-faced honeyeaters feeding, around 40% were feeding on nectar with 60% feeding on insects. The yellow-faced honeyeater feeds on insects by gleaning, and by sallying or catching insects in flight or probing in bark crevices. The insects eaten are primarily Diptera (flies, mosquitoes, maggots, gnats and midges), beetles and spiders. They feed as individuals, as pairs or as small groups of up to ten birds, and during migration in larger groups. They sometimes feed in large mixed-species foraging flocks composed predominately of insectivorous birds.
In April and May, before the autumn migration, the yellow-faced honeyeater increases its nectar consumption, which increases its body mass. The average body mass in late autumn of 17.5 grams (0.62 oz) is 13% higher than the average recorded between January and April, and the yellow-faced honeyeater begins the migration with good fat reserves.
The yellow-faced honeyeater breeds in monogamous pairs in a breeding season that extends from July to March. Migrating birds begin nesting later than sedentary birds. They nest solitarily in all-purpose territories that both parents defend against conspecifics and other species including thornbills, spinebills and silvereyes, although the male is involved in more aggressive interactions than the female. Within a breeding season females lay two or three clutches of eggs, re-nesting with the same partner in the same territory. Banded birds have been identified in the same territory for periods of up to five years.
The nest is built in the understorey shrubs, relatively close to the ground. Nests have been recorded in prickly coprosma (Coprosma quadrifida), Cassinia, tea-trees (Melaleuca), eucalypts, and acacias, as well as in garden shrubs. The nest is a fragile, transparent structure, cup-shaped, but swollen at the sides and narrower at the rim. The female builds the nest, but is often accompanied by the male as she gathers nesting material. Most nests are built of greenish material which varies with the location; in coastal areas grass is the primary material, while in mountain forests the nest is often covered with moss. One bird was recorded repeatedly flying between the nest and a koala 36 metres (118 ft) away and plucking the long hair near its ears to incorporate in the nest. The nests are very fine, with the eggs visible through the gauze-like walls, and they sometimes fall apart. They have been known to disintegrate with eggs and nestlings falling through the bottom.
The female undertakes the incubation alone. Eggs are oval, approximately 21 millimetres (0.83 in) long and 14 millimetres (0.55 in) wide, and pinkish white in colour with spots and blotches of dark reddish brown. The clutch size varies from one to three eggs, and eggs take around two weeks to hatch. Upon hatching, both parents feed the nestlings and remove faecal pellets. The chicks fledge after thirteen days, and leave the parental territory after a further two weeks. The success rate can be as low as 16% of eggs developing into fledged young, with nest failure, hot weather, heavy rain, human activity (including fungicide spraying and nest damage), egg destruction by brood parasites, and predation by brown snakes, cats and currawongs all recorded as contributing to brood failure. (Among the species that parasitize the nests of yellow-faced honeyeaters are fan-tailed cuckoos, brush cuckoos, pallid cuckoos, shining bronze cuckoos and Horsfield's bronze cuckoos.) The yellow-faced honeyeater rapidly nests again after both successful and failed breeding attempts.
A paternity analysis of yellow-faced honeyeater nestlings found that 10 of 18 nestlings were fathered by the male of the nesting pair, with clear evidence for extra-pair paternity in the case of the remaining 44%. This conflicts with the usual pattern, where genetic monogamy is linked to the characteristics of strong social pairing, essential paternal contributions to brood rearing, and to sexual monomorphism; characteristics exhibited by the yellow honeyeater.
Several ectoparasites which can affect both survival and reproductive fitness have been found on the yellow-faced honeyeater; the mites Ptilonyssus meliphagae and Ptilonyssus thymanzae and Ixodes species ticks.
In general, honeyeaters require extensive corridors of mature trees along their migratory routes, and flowering woodlands for nesting, so they are vulnerable to the effects of land clearing, grazing and weed infestations. The woodland habitat they prefer is considered an endangered ecological community. However, as it is common and widespread, the yellow-faced honeyeater is considered by the IUCN to be of least concern for conservation. A field experiment to determine whether yellow-faced honeyeater nests were less successful in fragmented habitats found nests closer to forest margins actually had a higher success rate than those deeper within the forest. While the yellow-faced honeyeater tends to nest away from the edge of forest remnants, experiments with natural and artificial nests at varying distances from the open areas showed no increase in the number of avian predators at the forest edge. The experiment results do not support the "ecological trap" and "predator influx" theories and contribute to a belief that fragmented habitats may not be as problematic as previously thought. In some areas the species is considered a pest because of its intrusion into orchards and urban gardens where it damages fruit.
- BirdLife International (2012). "Lichenostomus chrysops". IUCN Red List of Threatened Species. Version 2013.2. International Union for Conservation of Nature. Retrieved 26 November 2013.
- Latham, John (1801). Supplementum indicis ornithologici sive systematis ornithologiae (in Latin). London: Leigh & Sotheby. p. liv.
- Schodde, Richard; Dickinson, Edward C.; Steinheimer, Frank D.; Bock, Walter J. (2010). "The date of Latham's Supplementum Indicis Ornithologici: 1801 or 1802?". South Australian Ornithologist. Adelaide, S.A.: Birds SA. 35 (8): 231–235. ISSN 0038-2973.
- Gray, Jeannie; Fraser, Ian (2013). Australian Bird Names: A Complete Guide. Collingwood, Victoria: Csiro Publishing. p. 199. ISBN 978-0-643-10471-6.
- Australian Biological Resources Study (13 October 2014). "Subspecies Caligavis chrysops chrysops (Latham, 1801)". Australian Faunal Directory. Canberra, Australian Capital Territory: Department of the Environment, Water, Heritage and the Arts, Australian Government. Retrieved 7 January 2017.
- Gardner, J.L.; Trueman, J. W. H.; Ebert, D.; Joseph, L.; Magrath, R. D. (2010). "Phylogeny and evolution of the Meliphagoidea, the largest radiation of Australian songbirds". Molecular Phylogenetics and Evolution. Elsevier. 55 (3): 1087–1102. doi:10.1016/j.ympev.2010.02.005. ISSN 1055-7903. PMID 20152917.
- . Nyári, Árpád S; Joseph, Leo (2011). "Systematic dismantlement of Lichenostomus improves the basis for understanding relationships within the honeyeaters (Meliphagidae) and the historical development of Australo-Papuan bird communities". Emu. Melbourne, Vic.: CSIRO. 111 (3): 202–211. doi:10.1071/MU10047.
- Higgins, Christidis & Ford 2008, p. 597.
- White, John (1790). Journal of a Voyage to New South Wales with sixty-five plates of nondescript animals, birds, lizards, serpents, curious cones of trees and other natural productions. p. 161.
- Higgins, Peter & Steele 2001, p. 724.
- Officer 1965, p. 50.
- Higgins, Peter & Steele 2001, p. 725.
- Ford, Hugh A.; Paton, David C. (1976). "Resource partitioning and competition in honeyeaters of the genus Meliphaga". Australian Journal of Ecology. 1 (4): 281–287. doi:10.1111/j.1442-9993.1976.tb01118.x.
- Higgins, Peter & Steele 2001, p. 728.
- Clarke, Michael; Schipper, Clinton; Boulton, Rebecca; Ewen, John (2003). "The social organization and breeding behaviour of the Yellow-faced Honeyeater Lichenostomus chrysops– a migratory passerine from the Southern Hemisphere". Ibis. 145 (4): 611–623. doi:10.1046/j.1474-919X.2003.00203.x.
- Higgins, Peter & Steele 2001, p. 727.
- Liddy, J. (1996). "Autumnal migration of the Yellow-faced Honeyeater". Emu. Melbourne, Vic: CSIRO. 66 (2): 87–103. doi:10.1071/MU966087.
- Munro, Ursula; Wiltschko, Roswitha (1993). "Clock-shift experiments with migratory Yellow-faced Honeyeaters, Lichenostomus chrysops (Meliphagidae), an Australian day-migrating bird". Journal of Experimental Biology. 181: 233–244.
- Munro, Ursula; Wiltschko, Wolfgang (1993). "Magnetic compass orientation in the yellow-faced honeyeater, Lichenostomus chrysops, a day migrating bird from Australia". Behavioral Ecology and Sociobiology. 32 (2): 141–145. doi:10.1007/BF00164047.
- Wilson, S.J. (1963). "Mist netting migrating Yellow-faced Honeyeaters". The Australian Bird Bander. Sydney, NSW: The Australian Bird Study Association. 1: 53–59. ISSN 0004-8747.
- Keast, A. (1968). "Seasonal movement in the Australian honeyeaters (Meliphagidae) and their ecological significance". Emu. Melbourne, Vic.: CSIRO. 67 (2): 159–209. doi:10.1071/MU967159.
- Munro, Ursula (1999). "Adaptations to a migratory lifestyle: An Australian perspective". In Adams, N.J.; Slotow, R.H. Proceedings of the 22nd International Ornithological Congress. Johannesburg: BirdLife South Africa. pp. 956–978. Retrieved 25 November 2011.
- Higgins, Peter & Steele 2001, p. 730.
- Bounds, Jenny (1996). "Lone Fuscous and Yellow-faced Honeyeaters keeping company". Canberra Bird Notes. Canberra, ACT: Canberra Ornithologists Group. 21 (1): 14. ISSN 0314-8211.
- Higgins, Peter & Steele 2001, p. 731.
- Munro 2003, p. 148.
- Higgins, Peter & Steele 2001, p. 732.
- Higgins, Peter & Steele 2001, p. 733.
- Higgins, Peter & Steele 2001, p. 734.
- Cody, M.L. (1991). "Honeyeater plucks koala for nest material". Emu. Melbourne, Vic: CSIRO. 91 (2): 125–126. doi:10.1071/MU9910125.
- Beruldsen 1980, p. 371.
- Higgins, Peter & Steele 2001, p. 735.
- Boulton, R. L; Cassey, P.; Schipper, C.; Clarke, M. F. (2003). "Nest site selection by Yellow-faced Honeyeaters Lichenostomus chrysops". Journal of Avian Biology. Blackwell. 34 (3): 267–274. doi:10.1034/j.1600-048X.2003.03062.x. ISSN 0908-8857.
- Ewen, John G.; Ciborowski, Kate L.; Clarke, Rohan H.; Boulton, Rebecca L.; Clarke, Michael F. (2008). "Evidence of extra-pair paternity in two socially monogamous Australian passerines: the Crescent Honeyeater and the Yellow-faced Honeyeater". Emu. 108 (2): 133–37. doi:10.1071/MU07040.
- Higgins, Peter & Steele 2001, p. 1262.
- Boulton, Rebecca L ; Clarke, Michael F (2003). "Do yellow-faced honeyeater (Lichenostomus chrysops) nests experience higher predation at forest edges?". Wildlife Research. 30 (2): 119–25. doi:10.1071/WR02055. Vancouver style error: punctuation (help)
- Beruldsen, Gordon (1980). A Field Guide to Nests and Eggs of Australian Birds. Adelaide, S.A.: Rigby. ISBN 0-7270-1202-9.
- Higgins, Peter; Peter, J.M.; Steele, W.K. (2001). "Lichenostomus chrysops Yellow-faced Honeyeater". Handbook of Australian, New Zealand and Antarctic Birds Volume 5, Tyrant-flycatchers to Chats. Melbourne, Vic: Oxford University Press. pp. 724–740. ISBN 0-19-553071-3.
- Higgins, Peter; Christidis, Les; Ford, Hugh (2008). "Family Meliphagidae (Honeyeaters)". In Josep, del Hoyo; Andrew, Elliott; David, Christie. Handbook of the Birds of the World. Volume 13, Penduline-tits to Shrikes. Barcelona: Lynx Edicions. pp. 597–598. ISBN 978-84-96553-45-3.
- Munro, Ursula (2003). "Life History and Ecophysical Adaptations to Migration in Australian Birds". In Berthold, Peter; Gwinner, Eberhard; Sonnenschein, E. Avian Migration. New York, N.Y.: Springer-Verlag. pp. 141–154. ISBN 3-540-43408-9.
- Officer, Hugh R. (1965). Australian Honeyeaters. Melbourne, Vic.: The Bird Observers Club, Melbourne. ISBN 0-909711-03-8.
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